Evidence map›Paper›PMID 37720499›Full record

ReviewTherapeutic advances in medical oncology2023

What is the ideal endpoint in early-stage immunotherapy neoadjuvant trials in lung cancer?

Robert B Cameron, Jacobi B Hines, Valter Torri, Luca Porcu, Jessica Donington, Christine M Bestvina, Everett Vokes, James M Dolezal, Alessandra Esposito, Marina C Garassino

Abstract readReview
In one paragraph

Review in Therapeutic advances in medical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Robert B CameronDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.
Jacobi B HinesDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.
Valter TorriDepartment of Oncology, Institute of Pharmacological Research 'Mario Negri', IRCCS, Milan, Italy.
Luca PorcuDepartment of Oncology, Institute of Pharmacological Research 'Mario Negri', IRCCS, Milan, Italy.
Jessica DoningtonDepartment of Surgery, Section Thoracic Surgery, University of Chicago, Chicago, IL, USA.
Christine M BestvinaDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.
Everett VokesDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.
James M DolezalDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.
Alessandra EspositoDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.ORCID https://orcid.org/0000-0003-0664-3122
Marina C GarassinoDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, 5841 S Maryland Avenue, Chicago, IL 60637, USA.

Funding

CLINICAL THERAPEUTICST32GM007019 · NIGMS · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell, MARK J RATAIN · 1985 to 2026
$8.7M
NIGMS NIH HHS T32 GM007019
6 · The paper itself

Abstract

Numerous clinical trials investigating neoadjuvant immune checkpoint inhibitors (ICI) have been performed over the last 5 years. As the number of neoadjuvant trials increases, attention must be paid to identifying informative trial endpoints. Complete pathologic response has been shown to be an appropriate surrogate endpoint for clinical outcomes, such as event-free survival or overall survival, in breast cancer and bladder cancer, but it is less established for non-small-cell lung cancer (NSCLC). The simultaneous advances reported with adjuvant ICI make the optimal strategy for early-stage disease debatable. Considering the long time required to conduct trials, it is important to identify optimal endpoints and discover surrogate endpoints for survival that can help guide ongoing clinical research. Endpoints can be grouped into two categories: medical and surgical. Medical endpoints are measures of survival and drug activity; surgical endpoints describe the feasibility of neoadjuvant approaches at a surgical level as well as perioperative attrition and complications. There are also several exploratory endpoints, including circulating tumor DNA clearance and radiomics. In this review, we outline the advantages and disadvantages of commonly reported endpoints for clinical trials of neoadjuvant regimens in NSCLC.

Indexed as

chemoimmunotherapyendpointsimmunotherapyneoadjuvantpathologic response

Identifiers

PMID37720499
PMCPMC10504845

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.